FR2439222A1 - Azo dyes prepn. - by diazotising aromatic prim. amine and coupling with aryl:aliphatic, benzenoid, naphthalenic or heterocyclic cpd. - Google Patents
Azo dyes prepn. - by diazotising aromatic prim. amine and coupling with aryl:aliphatic, benzenoid, naphthalenic or heterocyclic cpd.Info
- Publication number
- FR2439222A1 FR2439222A1 FR7829508A FR7829508A FR2439222A1 FR 2439222 A1 FR2439222 A1 FR 2439222A1 FR 7829508 A FR7829508 A FR 7829508A FR 7829508 A FR7829508 A FR 7829508A FR 2439222 A1 FR2439222 A1 FR 2439222A1
- Authority
- FR
- France
- Prior art keywords
- coupling
- diazotising
- naphthalenic
- benzenoid
- prim
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B41/00—Special methods of performing the coupling reaction
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Azo dyes (I) are prepd. in aq. media by diazotising aromatic prim. amines at 20-50 degrees C and coupling at 20-90 degrees C and pH 0-13 with an arylaliphatic, benzenoid, naphthalenic or heterocyclic cpd. (I) can be used as acid, disperse, mordant, etc. dyes, or pigments. Diazotisation and coupling can be effected at relatively high temps. in conc. milieu in very short reaction times (seconds to minutes) and increased yields are obtd. Ice is no longer required generally or only very slightly. The vols. of water required for a given weight of (I) are much less than normal.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7829508A FR2439222A1 (en) | 1978-10-17 | 1978-10-17 | Azo dyes prepn. - by diazotising aromatic prim. amine and coupling with aryl:aliphatic, benzenoid, naphthalenic or heterocyclic cpd. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7829508A FR2439222A1 (en) | 1978-10-17 | 1978-10-17 | Azo dyes prepn. - by diazotising aromatic prim. amine and coupling with aryl:aliphatic, benzenoid, naphthalenic or heterocyclic cpd. |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2439222A1 true FR2439222A1 (en) | 1980-05-16 |
FR2439222B1 FR2439222B1 (en) | 1981-02-27 |
Family
ID=9213821
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7829508A Granted FR2439222A1 (en) | 1978-10-17 | 1978-10-17 | Azo dyes prepn. - by diazotising aromatic prim. amine and coupling with aryl:aliphatic, benzenoid, naphthalenic or heterocyclic cpd. |
Country Status (1)
Country | Link |
---|---|
FR (1) | FR2439222A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4988804A (en) * | 1987-11-10 | 1991-01-29 | Ciba-Geigy Corporation | Polyazo dyes obtained by successive coupling of H-acid and two further anilinic diazo components on resorcinol or the like |
CN106243005A (en) * | 2016-07-07 | 2016-12-21 | 山西大同大学 | 3,5 dimethyl sulphur-based 2,4 2 (4,4 ' dinitro azo phenylamino azo group) toluene and preparation method and application |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3681320A (en) * | 1970-01-13 | 1972-08-01 | Du Pont | Preparation of disazo j acid urea dyestuffs |
FR2138777A1 (en) * | 1971-05-21 | 1973-01-05 | Organickych Syntez | |
FR2309517A1 (en) * | 1975-04-29 | 1976-11-26 | Vyzk Ustav Organ Syntez | AUTOMATIC MANUFACTURING PROCESS OF DIAZOIC COMPOUNDS |
-
1978
- 1978-10-17 FR FR7829508A patent/FR2439222A1/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3681320A (en) * | 1970-01-13 | 1972-08-01 | Du Pont | Preparation of disazo j acid urea dyestuffs |
FR2138777A1 (en) * | 1971-05-21 | 1973-01-05 | Organickych Syntez | |
FR2309517A1 (en) * | 1975-04-29 | 1976-11-26 | Vyzk Ustav Organ Syntez | AUTOMATIC MANUFACTURING PROCESS OF DIAZOIC COMPOUNDS |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4988804A (en) * | 1987-11-10 | 1991-01-29 | Ciba-Geigy Corporation | Polyazo dyes obtained by successive coupling of H-acid and two further anilinic diazo components on resorcinol or the like |
CN106243005A (en) * | 2016-07-07 | 2016-12-21 | 山西大同大学 | 3,5 dimethyl sulphur-based 2,4 2 (4,4 ' dinitro azo phenylamino azo group) toluene and preparation method and application |
Also Published As
Publication number | Publication date |
---|---|
FR2439222B1 (en) | 1981-02-27 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
ST | Notification of lapse |